A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481596



Internal ID21139149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80114701..80117200hg38UCSC Ensembl
chr13:80688836..80691335hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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